US 12,287,321 B2
Optical multianalyte detection
Dena Marrinucci, San Diego, CA (US); Nicholas Haase, San Diego, CA (US); Ryan Morgan, San Diego, CA (US); Michael Adams, San Diego, CA (US); Derek Arndt, San Diego, CA (US); Graeme Cross, San Diego, CA (US); Jeffrey A. Hawkins, San Diego, CA (US); David Hecht, San Diego, CA (US); Johnny Steve Rachele, San Diego, CA (US); Roger Taylor, San Diego, CA (US); Scott Thompson, San Diego, CA (US); Kyoung-Ho Kim, San Diego, CA (US); David Luke McDonald, San Diego, CA (US); Michael White, San Diego, CA (US); and Kevin Yang, San Diego, CA (US)
Assigned to Truvian Sciences, Inc., San Diego, CA (US)
Filed by Truvian Sciences, Inc., San Diego, CA (US)
Filed on Sep. 8, 2023, as Appl. No. 18/464,185.
Prior Publication US 2025/0085271 A1, Mar. 13, 2025
Int. Cl. G01N 33/49 (2006.01); B01L 3/00 (2006.01); C12Q 1/6816 (2018.01); G01N 21/17 (2006.01); G01N 21/31 (2006.01); G01N 21/64 (2006.01)
CPC G01N 33/492 (2013.01) [B01L 3/502 (2013.01); C12Q 1/6816 (2013.01); G01N 21/6428 (2013.01); B01L 2200/04 (2013.01); B01L 2200/0642 (2013.01); B01L 2200/143 (2013.01); B01L 2200/16 (2013.01); B01L 2300/021 (2013.01); B01L 2300/0645 (2013.01); B01L 2300/0663 (2013.01); G01N 2021/1765 (2013.01); G01N 2021/3155 (2013.01); G01N 2021/6417 (2013.01); G01N 2021/6439 (2013.01)] 19 Claims
OG exemplary drawing
 
1. An optical method for detecting the presence of a target analyte in a sample, the method comprising: a) moving automatically a first portion of a whole blood sample from a support pack to a first well in a disk in a detection instrument and moving automatically a second portion of the whole blood sample from the support pack to a reaction well in the support pack, the disk comprising dried chemistries for processing the sample, plasma separation features configured to separate whole blood into plasma, and a hematocrit channel configured to execute the hematocrit assay, the support pack comprising the whole blood sample, pipette tips, buffers, a reagent for processing the sample, reagent preparation wells, and a monolayer assay device configured to operate as a hematology slide; b) separating by the detection instrument plasma from the first portion of the whole blood sample in the disk while simultaneously moving reagent in the support pack for processing the plasma generated in the disk and diluting the second portion of the whole blood sample in the support pack; c) moving automatically by the detection instrument the plasma generated from the first portion of the whole blood sample from the disk to the support pack; d) diluting by the detection instrument the plasma generated from the first portion of the whole blood sample in the support pack; e) moving automatically by the detection instrument the plasma generated from the first portion of the whole blood sample from the support pack to the disk; and f) optically detecting by the detection instrument the presence or absence of said first target analyte, the detection instrument comprising a laser and at least one of a spectrophotometer, or a camera.